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Ryo Taguchi

Showing results (141-150 of 154) with videos related to

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The Journal of Biological Chemistry|September 20, 2008
Analyses of group III secreted phospholipase A2 transgenic mice reveal potential participation of this enzyme in plasma lipoprotein modification, macrophage foam cell formation, and atherosclerosisHiroyasu Sato, Rina Kato, Yuki Isogai, et al.
The Journal of Biological Chemistry|January 27, 2011
Hair follicular expression and function of group X secreted phospholipase A2 in mouse skinKei Yamamoto, Yoshitaka Taketomi, Yuki Isogai, et al.
The Journal of Experimental Medicine|May 22, 2013
Lymphoid tissue phospholipase A2 group IID resolves contact hypersensitivity by driving antiinflammatory lipid mediatorsYoshimi Miki, Kei Yamamoto, Yoshitaka Taketomi, et al.
Cell Metabolism|June 10, 2014
The adipocyte-inducible secreted phospholipases PLA2G5 and PLA2G2E play distinct roles in obesityHiroyasu Sato, Yoshitaka Taketomi, Ayako Ushida, et al.
Hypertension (Dallas, Tex. : 1979)|January 9, 2013
Novel regulation of cardiac metabolism and homeostasis by the adrenomedullin-receptor activity-modifying protein 2 systemTakahiro Yoshizawa, Takayuki Sakurai, Akiko Kamiyoshi, et al.
Diabetologia|December 31, 2013
Hypothalamic SIRT1 prevents age-associated weight gain by improving leptin sensitivity in miceTsutomu Sasaki, Osamu Kikuchi, Mayumi Shimpuku, et al.
Cell|March 13, 2013
The lipid mediator protectin D1 inhibits influenza virus replication and improves severe influenzaMasayuki Morita, Keiji Kuba, Akihiko Ichikawa, et al.
Plos Pathogens|August 24, 2012
Self-enhancement of hepatitis C virus replication by promotion of specific sphingolipid biosynthesisYuichi Hirata, Kazutaka Ikeda, Masayuki Sudoh, et al.
Frontiers in Medicine|October 17, 2022
Factors associated with low prevalence of Fuchs' uveitis syndrome in JapanYu Yoneda, Yoshihiko Usui, Rie Tanaka, et al.
American Journal of Human Genetics|June 14, 2011
A congenital muscular dystrophy with mitochondrial structural abnormalities caused by defective de novo phosphatidylcholine biosynthesisSatomi Mitsuhashi, Aya Ohkuma, Beril Talim, et al.
Pageof 16

Showing results (141-150 of 154) with videos related to

Sort By:
Pageof 16
The Journal of Biological Chemistry|September 20, 2008
Analyses of group III secreted phospholipase A2 transgenic mice reveal potential participation of this enzyme in plasma lipoprotein modification, macrophage foam cell formation, and atherosclerosisHiroyasu Sato, Rina Kato, Yuki Isogai, et al.
The Journal of Biological Chemistry|January 27, 2011
Hair follicular expression and function of group X secreted phospholipase A2 in mouse skinKei Yamamoto, Yoshitaka Taketomi, Yuki Isogai, et al.
The Journal of Experimental Medicine|May 22, 2013
Lymphoid tissue phospholipase A2 group IID resolves contact hypersensitivity by driving antiinflammatory lipid mediatorsYoshimi Miki, Kei Yamamoto, Yoshitaka Taketomi, et al.
Cell Metabolism|June 10, 2014
The adipocyte-inducible secreted phospholipases PLA2G5 and PLA2G2E play distinct roles in obesityHiroyasu Sato, Yoshitaka Taketomi, Ayako Ushida, et al.
Hypertension (Dallas, Tex. : 1979)|January 9, 2013
Novel regulation of cardiac metabolism and homeostasis by the adrenomedullin-receptor activity-modifying protein 2 systemTakahiro Yoshizawa, Takayuki Sakurai, Akiko Kamiyoshi, et al.
Diabetologia|December 31, 2013
Hypothalamic SIRT1 prevents age-associated weight gain by improving leptin sensitivity in miceTsutomu Sasaki, Osamu Kikuchi, Mayumi Shimpuku, et al.
Cell|March 13, 2013
The lipid mediator protectin D1 inhibits influenza virus replication and improves severe influenzaMasayuki Morita, Keiji Kuba, Akihiko Ichikawa, et al.
Plos Pathogens|August 24, 2012
Self-enhancement of hepatitis C virus replication by promotion of specific sphingolipid biosynthesisYuichi Hirata, Kazutaka Ikeda, Masayuki Sudoh, et al.
Frontiers in Medicine|October 17, 2022
Factors associated with low prevalence of Fuchs' uveitis syndrome in JapanYu Yoneda, Yoshihiko Usui, Rie Tanaka, et al.
American Journal of Human Genetics|June 14, 2011
A congenital muscular dystrophy with mitochondrial structural abnormalities caused by defective de novo phosphatidylcholine biosynthesisSatomi Mitsuhashi, Aya Ohkuma, Beril Talim, et al.
Pageof 16